State
73,833 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.
Of the 23 recalls naming Northern Mariana Islands we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 18 (78%) are Severe.
Which agencies issued them
These figures cover only the 23 recalls whose distribution notice names Northern Mariana Islands specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Novel Laboratories is recalling 25,776 containers of Famotidine Oral Suspension because the product failed an impurity specification. The recall is classified as FDA Class III.
Mylan Pharmaceuticals is recalling Diltiazem HCl Extended Release Capsules because routine stability testing found high levels of a related compound.
Ford is recalling specific 2014 Focus, 2014 Escape, and 2015 Lincoln MKC vehicles because a fuel delivery module may crack, causing low fuel pressure and potential vehicle stalls.
Ford is recalling 2015 F-650 and F-750 SD trucks because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.
Mitsubishi is recalling 2010-2014 i-MiEV electric vehicles because the brake vacuum pump may stop functioning, potentially increasing stopping distance and crash risk.
Genera is recalling specific aftermarket headlamp assemblies for 2013-2014 Acura ILX vehicles due to overheating risks that could cause smoke, melting, or fire.
Trimas is recalling specific Highland and Reese roof rack carriers because they may lack warning labels against using them with cargo bags or boxes.
Tray Vous is recalling snack and activity trays for strollers because the design poses a strangulation hazard to unharnessed children.
Gillig is recalling 231 model year 2014 Low Floor transit buses because a fuel filter defect may cause the engine to stall unexpectedly, increasing the risk of a crash.
New Flyer is recalling 2014 transit buses because a fuel filter defect may cause the engine to stall without warning, increasing the risk of a crash.
General Motors is recalling specific 2013-2014 Cadillac XTS and Chevrolet Impala vehicles because the air bag control module may be in manufacturing mode, preventing deployment in a crash.
American Woodcrafters is recalling about 1,900 Cottage Retreat II bunk beds sold at Havertys because side support rails can break, posing a fall hazard.
Baxter Healthcare is recalling 4,200 containers of 0.9% Sodium Chloride Injection because blue polyisoprene shavings were found inside the bag port tubes.
Natural Grocers by Vitamin Cottage is recalling Chunks of Energy products due to the potential presence of Salmonella.
Ben Venue Laboratories is recalling 7,172 vials of Cytarabine for Injection due to potential crimp defects that may affect sterility.
AngioDynamics is recalling Uni*Fuse Infusion Systems with Cooper Wire because they may contain a guidewire that is too long.
Ortho Development is recalling specific knee implant components because defective foil pouches allowed air to enter, potentially degrading the material properties of the implants.
Childrens Medical Ventures is recalling Gel-E Donut and Squishon 2 gel pillows because of visible mold. The mold was identified as Cladosporium and Penicillium fungi.
Goodman Company is recalling approximately 233,500 packaged terminal air conditioners and heat pumps because power cords can overheat, posing fire and burn risks.
Synthes, Inc. is recalling specific lots of the DePuy Synthes Craniomaxillofacial Distraction System because the devices may reverse after surgery.
Hospira Inc. is recalling 123,900 vials of Dobutamine Injection due to the presence of glass particulate matter and a discolored solution.
Fresenius Kabi USA, LLC is recalling 56,060 vials of Propranolol Hydrochloride Injection because the active ingredient supplier received citations for critical manufacturing deficiencies.
Hospira Inc. is recalling 844,300 vials of Propofol Injectable Emulsion because glass defects allowed metallic particulates to enter the solution.
Ortho Development is recalling various knee implant components because foil pouches failed to seal properly, allowing air to enter and potentially degrading the material properties of the implants.
Natural Grocers by Vitamin Cottage is recalling Organic Chunks of Energy Carob Supergreens due to the potential presence of Salmonella.